International safety notice
Urgent Field Safety Notice for Prestige II, Prestige VH, Prestige SI, Prestilix 1600X, Precision 500D, Flexmed, PROTEUS XR/A and SILHOUETTE VR by GE Healthcare
Germany / BfArM · DEU · Apr 30, 2019
Key facts
| Title | Urgent Field Safety Notice for Prestige II, Prestige VH, Prestige SI, Prestilix 1600X, Precision 500D, Flexmed, PROTEUS XR/A and SILHOUETTE VR by GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Prestige II, Prestige VH, Prestige SI, Prestilix 1600X, Precision 500D, Flexmed, PROTEUS XR/A and SILHOUETTE VR |
| Manufacturer | GE Healthcare |
| Models | NEV12301, A1767009, D1242801, CS1019RX01, M1469807, A2032101, M1478607, D4185515, RU2592RX01, A5157001, P4172816, C5129901 and 813 more |
| Date | Apr 30, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1